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Chorioretinopathy, Birdshot type
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal dominant beta2-microglobulinic amyloidosis
1 associated gene
No signs/symptoms info
Chorioretinopathy, Birdshot type
Autosomal dominant beta2-microglobulinic amyloidosis

HLA-A
(UniProt - OMIM)
 B2M
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HLA-A
(0.82)
B2M


Citations in the biomedical literature:


Chorioretinopathy, Birdshot type
HLA-A
Autosomal dominant beta2-microglobulinic amyloidosis
B2M



Chorioretinopathy, Birdshot type
Autosomal dominant beta2-microglobulinic amyloidosis

Classification (Orphanet):
- Rare eye disease
Classification (Orphanet):
- Rare genetic disease
- Rare systemic or rheumatologic disease
Classification (ICD10):
- Diseases of the eye and adnexa -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: normal
Type of inheritance: unknown
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
1 MeSH reference: C537630
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.